This application is based upon and claims the benefit of priority from prior Japanese Patent Application No. 2008-147121 filed on Jun. 4, 2008 in Japan, the entire contents of which are incorporated herein by reference.
1. Field of the Invention
The present invention relates to a method for manufacturing a semiconductor device.
2. Background Art
A demand for miniaturization of a semiconductor device is addressed until now by methods such as shortening of exposure wavelength and increase in NA (numeric aperture) of an exposure lens in a photolithography process. However, it is becoming difficult to address a demand for fast-paced further miniaturization of a semiconductor device by conventional methods such as shortening of exposure wavelength and increase in NA of an exposure lens.
Consequently, a technique called double patterning is being proposed. Briefly, this technique is an application of multiple exposure. For example, exposure is performed on a resist film once with a mask of a rough pattern. The mask is displaced and exposure is performed again. After that, development is performed.
In this technique, however, precision of alignment of an exposure apparatus at the time of multiple exposure is strictly requested and it is difficult to realize the technique in practice.
A method for forming a fine pattern of a silicon oxide film is also proposed (for example, Japanese Patent Laid-Open No. 1991-270227).
The method will be described as follows.
First, a resist pattern is formed at low pitches on a substrate to be processed. The resist pattern itself has a width corresponding to a predetermined pitch.
Next, a silicon oxide film is formed so as to cover at least the resist pattern.
Further, the silicon oxide film is etched so that the silicon oxide film remains only on both sides of each of the resist patterns. A gap of a predetermined pitch is formed between the silicon oxide films on both sides of neighboring resist patterns.
Subsequently, the resist pattern sandwiched by the silicon oxide films is selectively removed to make the silicon oxide films on both sides remain. As a result, the remaining silicon oxide films are arranged at intervals of the predetermined pitch. That is, a fine pattern having an interval of the pitch which is the half of the low pitch of the initial resist pattern is formed in the silicon oxide film.
According to an aspect of an embodiment of the present invention, there is provided a method for manufacturing a semiconductor device, comprising: forming a resist film on a substrate and processing the resist film to be provided with openings to form a first resist pattern; forming additive-containing layers so that the additive-containing layers cover a surface of the first resist pattern, the additive-containing layers containing an additive that changes a state of the resist film from a non-soluble state to a soluble state for a developer; forming a first resin film in a state that the first resin film is buried in the openings of the first resist pattern, a state of the first resin film being changed from a non-soluble state to a soluble state for the developer when the first resin film contains the additive, and the openings of the first resist pattern being covered with the additive-containing layers; diffusing the additive into the first resist pattern and the first resin film, respectively, the first resist pattern being covered with the additive-containing layers and being medially-located to the additive-containing layers, and the first resin film being laterally-located to the additive-containing layers, to form first additive-diffusing portions in the first resist pattern and second additive-diffusing portions in the first resin film, the first and second additive-diffusing portions being able to be solved in the developer; and removing the first additive-diffusing portions and the second additive-diffusing portions with the developer, to form a second resist pattern made of remaining portions in the first resist pattern and remaining portions in the first resin film.
A method for forming a pattern of the first embodiment of the present invention will be described below with reference to
(Formation of Resist Pattern)
On a substrate 1 as a member to be processed, an ArF organic antireflection film (trade name: ARC29A manufactured by Nissan Chemical Industries, Ltd.) by spin coating. Next, the resultant is baked under conditions of temperature of 215 C and one minute to form an ArF organic antireflection film (antireflection film) 2a having a thickness of 80 nm (refer to
After that, on the ArF organic antireflection film 2a, an ArF positive resist having a nature of changing from a non-soluble state to a soluble state for an alkaline developer by containing an acid additive is coated by spin coating. The resultant is further baked under conditions of temperature of 130 C and one minute, thereby forming an ArF positive resist film 5a having a thickness of 150 nm on the ArF organic antireflection film 2a (refer to
The ArF positive resist film 5a is exposed using a halftone mask 4 having transmittance of 6% under conditions of NA=0.85 and ⅔ annular illumination in an ArF excimer laser exposure apparatus (refer to
Subsequently, the halftone mask 4 is removed and the resultant is baked under conditions of temperature of 100 C and one minute (refer to
Development is performed with a tetramethylammonium hydroxide (TMAH) solution of 2.38 weight %, thereby forming an ArF positive resist pattern (first resist pattern) 5b of 110 nm and 1:1 L/S (refer to
(Addition of Additive)
An application solution (second application solution) containing an acid additive and a water-soluble resin material (second resin film material) is applied so as to bury openings of the ArF positive resist pattern 5b and cover the surface of the ArF positive resist pattern 5b. After that, the resultant is baked under conditions of temperature of 100 C and one minute to form a water-soluble resin film (second resin film) 6a (refer to
At this time, a mixing reaction occurs on an interface between the ArF positive resist pattern 5b and the water-soluble resin film 6a to form additive-containing layers 6M containing the acid additive (refer to
Unreacted portions 6NM in the water-soluble resin film 6a with the ArF positive resist pattern 5b are removed by water washing, and the additive-containing layers 6M are left on the surface of the ArF positive resist pattern 5b (refer to
(Diffusion of Acid Additive)
Next, a solution (first application solution) containing a resin (first resin film material) and an alcohol solvent (first solvent) is applied on the ArF positive resist pattern 5b covered with the additive-containing layers 6M. The resin has a nature of changing from a non-soluble state to a soluble state for an alkaline developer by containing an acid additive. The resin is a chemically amplified resist which does not contain a photo-acid-generating agent. The alcohol solvent may be properly selected from solvents which do not make the resist dissolved. For example, as an alcohol solvent, it is preferable to use alcohols such as a known solvent for a liquid immersion protection film. More preferably, a monohydroxy alcohol is used. Most preferably, a monohydroxy alcohol having a carbon number of 1 to 10 is used.
As a result, as understood from
The solution is baked under conditions of 100 C and one minute to form a resin film 9a (first resin film) from the solution. The resin film 9a has a nature of changing from a non-soluble state to a soluble state for an alkaline developer by containing an acid additive (refer to
Subsequently, the resultant is baked under conditions of 120 C and two minutes, and the acid additive unevenly distributed in the additive-containing layers 6M is diffused to both sides of the additive-containing layers 6M in
Portions (first additive-diffusing portions) 5b1 in the ArF positive resist pattern 5b and portions (second additive-diffusing portions) 9a1 in the resin film 9a containing the acid additive by the diffusion have a nature that they can be solved in an alkali developer (refer to
(Second Pattern Forming Process)
When developing process is performed with the alkaline developer, the portions (first additive-diffusing portions) 5b1 in the ArF positive resist pattern 5b and the portions (second additive-diffusing portions) 9a1 in the resin film 9a containing the acid additive are dissolved (refer to
That is, as shown in
As described above, according to the first embodiment of the present invention, the fine resist pattern can be easily formed.
A second embodiment of the present invention will be described below.
The second embodiment is different from the first embodiment with respect to the point that the resin film (first resin film) 9a is planarized by CMP (Chemical Mechanical Polish) (refer to
The point is employed in the second embodiment for the following reason.
As shown in
The second embodiment of the present invention will be described below with reference to
The processes shown in
First, as shown in
After that, the process shown in
As described above, in the second embodiment of the present invention, a fine resist pattern having a predetermined shape can be easily formed.
Additional advantages and modifications will readily occur to those skilled in the art.
Therefore, the invention in its broader aspects is not limited to the specific details and representative embodiments shown and described herein. Accordingly, various modifications may be made without departing from the spirit or scope of the general inventive concepts as defined by the appended claims and their equivalents.
Number | Date | Country | Kind |
---|---|---|---|
2008-147121 | Jun 2008 | JP | national |
Number | Name | Date | Kind |
---|---|---|---|
6486058 | Chun | Nov 2002 | B1 |
6558053 | Shigemori et al. | May 2003 | B2 |
6663761 | Kamijima | Dec 2003 | B2 |
6740479 | Loccufier et al. | May 2004 | B2 |
6916594 | Bok et al. | Jul 2005 | B2 |
7141177 | Tanaka | Nov 2006 | B2 |
7147985 | Yueh et al. | Dec 2006 | B2 |
7226726 | Kanda | Jun 2007 | B2 |
7335464 | Takano et al. | Feb 2008 | B2 |
7358037 | Cheng | Apr 2008 | B2 |
7527918 | Kondoh et al. | May 2009 | B2 |
7662542 | Shiobara et al. | Feb 2010 | B2 |
7799503 | Brodsky et al. | Sep 2010 | B2 |
7851139 | Shiobara et al. | Dec 2010 | B2 |
20060003601 | Sugeta et al. | Jan 2006 | A1 |
20060127816 | Kang et al. | Jun 2006 | A1 |
20070077524 | Koh et al. | Apr 2007 | A1 |
20080044759 | Ishibashi et al. | Feb 2008 | A1 |
20090220892 | Iwao et al. | Sep 2009 | A1 |
20090258318 | Chan | Oct 2009 | A1 |
20100183851 | Cao et al. | Jul 2010 | A1 |
20100330498 | Bae et al. | Dec 2010 | A1 |
Number | Date | Country |
---|---|---|
1152036 | Nov 2001 | EP |
1223470 | Jul 2002 | EP |
03-270227 | Dec 1991 | JP |
2004077951 | Mar 2004 | JP |
Number | Date | Country | |
---|---|---|---|
20090305167 A1 | Dec 2009 | US |